Variant report

Variant	rs73262648
Chromosome Location	chr8:68378094-68378095
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10091514	0.82[EUR][1000 genomes]
rs10100536	0.82[EUR][1000 genomes]
rs1393897	0.81[ASN][1000 genomes]
rs1566769	0.85[ASN][1000 genomes]
rs16933277	0.82[EUR][1000 genomes]
rs28502563	0.82[EUR][1000 genomes]
rs4386963	0.81[ASN][1000 genomes]
rs57070848	0.85[ASN][1000 genomes]
rs57438989	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57714056	0.81[ASN][1000 genomes]
rs58637111	0.84[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs59607772	0.81[ASN][1000 genomes]
rs60606572	0.87[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs61220075	0.81[ASN][1000 genomes]
rs61403252	0.82[EUR][1000 genomes]
rs6415606	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6472300	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6472301	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6472302	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6472303	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6472306	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6472307	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6472308	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6988019	0.82[EUR][1000 genomes]
rs6992371	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7005010	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7009065	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73258696	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73258699	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73262605	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73262624	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73262636	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73262638	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73262665	0.85[ASN][1000 genomes]
rs73262669	0.85[ASN][1000 genomes]
rs73262675	0.85[ASN][1000 genomes]
rs73262680	0.81[ASN][1000 genomes]
rs73262681	0.85[ASN][1000 genomes]
rs73262685	0.85[ASN][1000 genomes]
rs73262686	0.85[ASN][1000 genomes]
rs73262688	0.85[ASN][1000 genomes]
rs73262691	0.81[ASN][1000 genomes]
rs73262695	0.81[ASN][1000 genomes]
rs73262696	0.81[ASN][1000 genomes]
rs7815213	0.85[ASN][1000 genomes]
rs7824691	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7839073	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7842960	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7844794	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752263	chr8:68170946-68788493	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1024135	chr8:68235792-68629789	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv539642	chr8:68235792-68629789	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	esv2752264	chr8:68244546-68647201	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:68370200-68390200	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr8:68373200-68379400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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